Labverity
Facility profile

Boiron

Drug product manufacturing · Montevrain · France

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed3 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

LabelManufacture
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Nov 29, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Warning Letter · Sep 2023

Within five years · review the action and follow-up.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history3 inspection records

FDA inspection history

3 records, Jan 2015 – Nov 2024 · 1 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 29, 2024VAIDrug Quality Assurance2025
Jun 19, 2018NAIDrug Quality Assurance2018
Jan 30, 2015VAIDrug Quality AssuranceYes2015

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Sep 11, 2023Warning Letter · CDER
Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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